Canonical Allele Identifier: CA2243307028
Gene: SRR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.2313020G= , CM000679.2:g.2313020G= GRCh38
NC_000017.10:g.2216314G= , CM000679.1:g.2216314G= GRCh37
NC_000017.9:g.2163064G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344595.10:c.-4-2537G= MANE Select ENSP00000339435.5:n.-4-2537G=
ENST00000344595.9:c.-4-2537G= ENSP00000339435.5:n.-4-2537G=
ENST00000570662.2:c.-4-2537G= ENSP00000460581.2:n.-4-2537G=
ENST00000572709.5:c.-4-2537G= ENSP00000458814.1:n.-4-2537G=
ENST00000574987.1:c.-279-4850G= ENSP00000461343.1:n.-279-4850G=
ENST00000575840.5:c.-4-2537G= ENSP00000461589.1:n.-4-2537G=
ENST00000576620.5:c.-4-2537G= ENSP00000461125.1:n.-4-2537G=
ENST00000576848.1:c.-85+9003G= ENSP00000476682.1:n.-85+9003G=
NM_001304803.1:c.-279-4850G= NP_001291732.1:n.-279-4850G=
NM_021947.2:c.-4-2537G= NP_068766.1:n.-4-2537G=
XM_006721565.2:c.-4-2537G= XP_006721628.1:n.-4-2537G=
XM_006721566.2:c.-4-2537G= XP_006721629.1:n.-4-2537G=
XM_011523974.1:c.-4-2537G= XP_011522276.1:n.-4-2537G=
XM_011523975.1:c.-4-2537G= XP_011522277.1:n.-4-2537G=
XM_006721565.3:c.-4-2537G= XP_006721628.1:n.-4-2537G=
XM_006721566.3:c.-4-2537G= XP_006721629.1:n.-4-2537G=
XM_011523974.3:c.-4-2537G= XP_011522276.1:n.-4-2537G=
NM_021947.3:c.-4-2537G= MANE Select NP_068766.1:n.-4-2537G=